An in vitro assessment of the antibacterial properties and cytotoxicity of nanoparticulate silver bone cement

被引:733
作者
Alt, V
Bechert, T
Steinrücke, P
Wagener, M
Seidel, P
Dingeldein, E
Domann, E
Schnettler, R
机构
[1] Univ Giessen, Dept Trauma Surg, D-35385 Giessen, Germany
[2] Bio Gate, D-90411 Nurnberg, Germany
[3] Fraunhofer Inst Mfg & Adv Mat, D-28359 Bremen, Germany
[4] Coripharm, D-64807 Dieburg, Germany
[5] Univ Giessen, Inst Med Microbiol, D-35392 Giessen, Germany
关键词
nanoparticle; bone cement; polymethylmetacrylate; antibacterial; antimicrobial; arthroplasty;
D O I
10.1016/j.biomaterials.2003.10.078
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Infections with multiresistant bacteria have become a serious problem in joint arthroplasty. This study reports about in vitro antibacterial activity against multiresistant bacteria and in vitro cytotoxicity of polymethylmetacrylate bone cement loaded with metallic silver particles with a size of 5-50 nm called NanoSilver. In vitro antibacterial activity against S. epidermidis, methicillin-resistant S. epidermidis (MRSE), and methicillin-resistant S. aureus (MRSA) was studied by microplate proliferation tests. Quantitative elution testing and qualitative ongrowth of human osteoblasts was done to study in vitro cytotoxicity. Only NanoSilver cement showed high-antibacterial activity against all strains, including MRSE and MRSA. Gentamicin cement was not effective against MRSA and MRSE due to the high-level gentamicin resistance of the tested strains. Plain cement did not inhibit proliferation of any strains. There was no significant difference regarding in vitro cytotoxicty between NanoSilver and the non-toxic control. Cytotoxicity of cement loaded with silver salts made this kind of silver unsuitable for all day clinical use in the past. This new form of silver called NanoSilver was free of in vitro cytotoxicity and showed high effectiveness against multiresistant bacteria. If the results can be confirmed in vivo NanoSilver may have a high interest in joint arthroplasty. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4383 / 4391
页数:9
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